Brexpiprazole
ANDA 213692, held by Teva Pharms USA Inc. Brexpiprazole.
- First approved: Aug 11, 2022
- Review: Standard
- Supplements approved: 0
- Complete response letters: 0
Approvals and New Uses
The original application and every efficacy supplement, newest first| Date | Submission | Status | Documents |
|---|---|---|---|
| Aug 11, 2022 | Original application | Approved |
Products
6 strengths and forms| Product | Active ingredient | Marketing |
|---|---|---|
| Brexpiprazole0.25MG · tablet;oral | Brexpiprazole | Discontinued |
| Brexpiprazole0.5MG · tablet;oral | Brexpiprazole | Discontinued |
| Brexpiprazole1MG · tablet;oral | Brexpiprazole | Discontinued |
| Brexpiprazole2MG · tablet;oral | Brexpiprazole | Discontinued |
| Brexpiprazole3MG · tablet;oral | Brexpiprazole | Discontinued |
| Brexpiprazole4MG · tablet;oral | Brexpiprazole | Discontinued |
Identifiers
- Application
- ANDA 213692
- Drugs@FDA
- Overview at FDA
- Company
- Teva Pharmaceuticals USA
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed weekly; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters